Literature DB >> 21529936

The effect of polymer architecture, composition, and molecular weight on the properties of glycopolymer-based non-viral gene delivery systems.

Marya Ahmed1, Ravin Narain.   

Abstract

Although a variety of non-viral gene delivery vectors has been synthesized and used for gene delivery purposes, well-defined glycopolymer-based gene delivery carriers is not well explored. Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization technique allows successful and facile synthesis of cationic glycopolymers containing pendant sugar moieties in the absence of protecting group chemistry. A library of cationic glycopolymers of pre-determined molar masses and narrow polydispersities ranging from 3 to 30 kDa has been synthesized using RAFT polymerization technique. These polymers differ from each other in their architectures (block versus random), molecular weights, and monomer ratios (carbohydrate to cationic segment). It is shown that the above-mentioned parameters can largely affect the toxicity, DNA condensation ability and gene delivery efficacy of these polymers. Statistical copolymers of high degree of polymerization are found to be the ideal vector for gene delivery purposes. These statistical copolymers show lower toxicity and higher gene expression in the presence and absence of serum, as compared to the corresponding diblock copolymers. This is the first example of well-defined synthetic glycopolymers as DNA carriers that works both in the presence and absence of serum proteins. The critical composition of carbohydrate segment in copolymers for enhanced gene delivery and low toxicity was determined and an increase in carbohydrate residues in copolymers resulted in a decrease in transfection efficiencies of these polymers. The effect of serum proteins on statistical and diblock copolymer based polyplexes and hence gene delivery efficacy was studied. The results showed that the diblock copolymer-based polyplexes showed lower interactions with serum proteins, lower cellular uptake and very low gene expression in both Hep G2 and Hela cells in comparison to statistical copolymers.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21529936     DOI: 10.1016/j.biomaterials.2011.03.082

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  13 in total

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2.  Uptake and transfection with polymeric nanoparticles are dependent on polymer end-group structure, but largely independent of nanoparticle physical and chemical properties.

Authors:  Joel C Sunshine; Daniel Y Peng; Jordan J Green
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3.  Application of living free radical polymerization for nucleic acid delivery.

Authors:  David S H Chu; Joan G Schellinger; Julie Shi; Anthony J Convertine; Patrick S Stayton; Suzie H Pun
Journal:  Acc Chem Res       Date:  2012-01-13       Impact factor: 22.384

4.  Cationic Glycopolyelectrolytes for RNA Interference in Tick Cells.

Authors:  Kelli A Stockmal; Latoyia P Downs; Ashley N Davis; Lisa K Kemp; Shahid Karim; Sarah E Morgan
Journal:  Biomacromolecules       Date:  2021-11-18       Impact factor: 6.988

5.  Reconfiguring the architectures of cationic helical polypeptides to control non-viral gene delivery.

Authors:  Lichen Yin; Ziyuan Song; Kyung Hoon Kim; Nan Zheng; Haoyu Tang; Hua Lu; Nathan Gabrielson; Jianjun Cheng
Journal:  Biomaterials       Date:  2012-12-31       Impact factor: 12.479

6.  Influence of histidine incorporation on buffer capacity and gene transfection efficiency of HPMA-co-oligolysine brush polymers.

Authors:  Julie Shi; Joan G Schellinger; Russell N Johnson; Jennifer L Choi; Brian Chou; Ersilia L Anghel; Suzie H Pun
Journal:  Biomacromolecules       Date:  2013-05-20       Impact factor: 6.988

7.  Structural behavior of amphiphilic polyion complexes interacting with saturated lipid membranes investigated by coarse-grained molecular dynamic simulations.

Authors:  Daniel G Angelescu
Journal:  RSC Adv       Date:  2020-10-26       Impact factor: 4.036

8.  Investigating the effects of block versus statistical glycopolycations containing primary and tertiary amines for plasmid DNA delivery.

Authors:  Dustin Sprouse; Theresa M Reineke
Journal:  Biomacromolecules       Date:  2014-06-20       Impact factor: 6.988

9.  Influence of oligospermines architecture on their suitability for siRNA delivery.

Authors:  Maha Elsayed; Vincent Corrand; Vidula Kolhatkar; Yuran Xie; Na Hyung Kim; Rohit Kolhatkar; Olivia M Merkel
Journal:  Biomacromolecules       Date:  2014-03-04       Impact factor: 6.988

10.  Glucose-containing diblock polycations exhibit molecular weight, charge, and cell-type dependence for pDNA delivery.

Authors:  Yaoying Wu; Miao Wang; Dustin Sprouse; Adam E Smith; Theresa M Reineke
Journal:  Biomacromolecules       Date:  2014-04-25       Impact factor: 6.988

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